De novo ATP1A3 variants cause polymicrogyria
Miyatake, S; Kato, M; Kumamoto, T; Hirose, T; Koshimizu, E; Matsui, T; Takeuchi, H; Doi, H; Hamada, K; Nakashima, M; Sasaki, K; Yamashita, A; Takata, A; Hamanaka, K; Satoh, M; Miyama, T; Sonoda, Y; Sasazuki, M; Torisu, H; Hara, T; Sakai, Y; Noguchi, Y; Miura, M; Nishimura, Y; Nakamura, K; Asai, H; Hinokuma, N; Miya, F; Tsunoda, T; Togawa, M; Ikeda, Y; Kimura, N; Amemiya, K; Horino, A; Fukuoka, M; Ikeda, H; Merhav, G; Ekhilevitch, N; Miura, M; Mizuguchi, T; Miyake, N; Suzuki, A; Ohga, S; Saitsu, H; Takahashi, H; Tanaka, F; Ogata, K; Ohtaka-Maruyama, C; Matsumoto, N
Matsumoto, N (corresponding author), Yokohama City Univ, Grad Sch Med, Dept Human Genet, Yokohama, Kanagawa 2360004, Japan.
SCIENCE ADVANCES, 2021; 7 (13):